HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812193Generated: October 26, 2026
HCID 86647061, compound → N-(5-amino-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide
https://huagongshe.com/reaction/1812193
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86647061 | HCID 86647061 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(5-amino-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide | HCID 71480919 | 80.2% |
Reaction Steps
A solution of N-(2-chloro-5-(diphenylmethyleneamino)pyridin-3-yl)-4-fluorobenzenesulfonamide (0.520 g, 1.116 mmol) in THF (8 mL) and hydrochloric acid, 2 N (J. T. Baker) (0.837 mL, 1.674 mmol) was stirred at rt in a sealed tube for 30 min. The reaction mixture was partitioned between EtOAc and sat. NaHCO3. The aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layers were dried over MgSO4 and concentrated. The crude product was purified by column chromatography (80 g, 20% to 40% acetone in hexanes) to give the product as a yellow solid (0.270 g). m/z (ESI, +ve ion) 302.0 (M+H)+. 1H NMR (300 MHz, CDCl3) δ 7.80 (dd, J=8.77, 4.97 Hz, 2H); 7.61 (d, J=2.63 Hz, 1H); 7.34 (d, J=2.48 Hz, 1H); 7.16 (t, J=8.48 Hz, 2H); 6.82 (br. s., 1H); 3.84 (br. s., 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362241B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-2340a321e4cd43a9ac5c8c8fd03a0020 |
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| Source note | uspto-grants-2013_01 |
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